← Back to catalogue

Fogarty

FDA UDI

Class II (US FDA UDI)

by Edwards Lifesciences LLC

Identity

Trade Name
FOGARTY FDA UDI
Generic Name
Intravascular occluding balloon catheter, image-guided FDA UDI
Device Name
FOGARTY OCCLUSION CATHETER 8/22F 80CM FDA UDI
Model / Reference
62080822F FDA UDI
Description
FOGARTY OCCLUSION CATHETER 8/22F 80CM FDA UDI

Identifiers

Catalog Number
62080822F FDA UDI
Primary DI / UDI-DI
00690103043754 FDA UDI
510(k) Number
K093911 FDA UDI
K152762 FDA UDI
FDA Product Code
MJN FDA UDI
GMDN Term
Intravascular occluding balloon catheter, image-guided FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intravascular occluding balloon catheter, image-guided

Fogarty by Edwards Lifesciences LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravascular occluding balloon catheter, image-guided.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 6331ac5c-75cf-4165-bdc3-4da0ad1b54c4 38 fields · synced Jun 8, 2026